Canonical Allele Identifier: CA1899313850
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313460A= , CM000672.2:g.30313460A= GRCh38
NC_000010.10:g.30602389A= , CM000672.1:g.30602389A= GRCh37
NC_000010.9:g.30642395A= NCBI36
NG_028096.1:g.40879T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*149T= MANE Select ENSP00000263063.3:n.*149T=
ENST00000263063.8:c.*149T= ENSP00000263063.3:n.*149T=
ENST00000488290.5:n.3653T=
NM_018109.3:c.*149T= NP_060579.3:n.*149T=
NM_018109.4:c.*149T= MANE Select NP_060579.3:n.*149T=